微管多聚谷氨酸化是微管功能的调节剂,可导致神经退行性变。

Tubulin polyglutamylation, a regulator of microtubule functions, can cause neurodegeneration.

机构信息

Institut Curie, PSL Research University, CNRS UMR3348, F-91401 Orsay, France; Université Paris-Saclay, CNRS UMR3348, F-91401 Orsay, France.

Institut Curie, PSL Research University, CNRS UMR3348, F-91401 Orsay, France; Université Paris-Saclay, CNRS UMR3348, F-91401 Orsay, France.

出版信息

Neurosci Lett. 2021 Feb 16;746:135656. doi: 10.1016/j.neulet.2021.135656. Epub 2021 Jan 19.

Abstract

Neurodegenerative diseases lead to a progressive demise of neuronal functions that ultimately results in neuronal death. Besides a large variety of molecular pathways that have been linked to the degeneration of neurons, dysfunctions of the microtubule cytoskeleton are common features of many human neurodegenerative disorders. Yet, it is unclear whether microtubule dysfunctions are causative, or mere bystanders in the disease progression. A so-far little explored regulatory mechanism of the microtubule cytoskeleton, the posttranslational modifications of tubulin, emerge as candidate mechanisms involved in neuronal dysfunction, and thus, degeneration. Here we review the role of tubulin polyglutamylation, a prominent modification of neuronal microtubules. We discuss the current understanding of how polyglutamylation controls microtubule functions in healthy neurons, and how deregulation of this modification leads to neurodegeneration in mice and humans.

摘要

神经退行性疾病导致神经元功能的进行性丧失,最终导致神经元死亡。除了与神经元变性相关的多种分子途径外,微管细胞骨架的功能障碍也是许多人类神经退行性疾病的共同特征。然而,微管功能障碍是疾病进展的原因,还是仅仅是旁观者尚不清楚。微管细胞骨架的一个迄今为止研究较少的调节机制,即微管蛋白的翻译后修饰,作为涉及神经元功能障碍,进而导致变性的候选机制出现。在这里,我们回顾了微管蛋白多聚谷氨酸化的作用,这是神经元微管的一个重要修饰。我们讨论了目前对多聚谷氨酸化如何控制健康神经元中微管功能的理解,以及这种修饰的失调如何导致小鼠和人类的神经退行性变。

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